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Kyriaki Kekou

Showing results (1-10 of 27) with videos related to

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Turkish Journal of Orthodontics|April 4, 2022
Orofacial Manifestations Associated with Muscular Dystrophies: A ReviewPetros Papaefthymiou, Kyriaki Kekou, Fulya Özdemir
Movement Disorders : Official Journal of the Movement Disorder Society|September 27, 2016
Analysis of a founder mutation in the TH gene in a cohort of greek patients with Parkinson's diseaseRoser Pons, Kyriaki Kekou, Roubina Antonellou, et al.
The Journal of Molecular Diagnostics : JMD|February 26, 2010
SURVEYOR on the spot: strengths and weaknesses in molecular diagnosticsNikolaos Vogiatzakis, Kyriaki Kekou, Christalena Sophocleous, et al.
Molecular Biotechnology|August 13, 2013
Screening human genes for small alterations performing an enzymatic cleavage mismatched analysis (ECMA) protocolNikolaos Vogiatzakis, Kyriaki Kekou, Christalena Sophocleous, et al.
Neurology India|September 15, 2016
Myotonic dystrophy type 2 presenting as inflammatory myopathyConstantinos Papadopoulos, Grigoris Panagopoulos, Kyriaki Kekou, et al.
Neurology India|July 7, 2017
Author's Reply: Myotonic dystrophy: The occurrence of early-onset cataractConstantinos Papadopoulos, Grigoris Panagopoulos, Kyriaki Kekou, et al.
Molecular Biotechnology|October 24, 2007
Screening human genes for small alterations performing an enzymatic cleavage mismatched analysis (ECMA) protocolNikolaos Vogiatzakis, Kyriaki Kekou, Christalena Sophocleous, et al.
The Neurologist|July 18, 2015
Caveolinopathies in GreeceConstantinos Papadopoulos, George K Papadimas, Kyriaki Kekou, et al.
Pediatric Diabetes|November 13, 2021
Homozygosity of the Z-2 polymorphic variant in the aldose reductase gene promoter confers increased risk for neuropathy in children and adolescents with Type 1 diabetesDimitra Kallinikou, Charalampos Tsentidis, Kyriaki Kekou, et al.
Hormone Research|January 31, 2004
Tall stature, insulin resistance, and disturbed behavior in a girl with the triple X syndrome harboring three SHOX genes: offspring of a father with mosaic Klinefelter syndrome but with two maternal X chromosomesChristina Kanaka-Gantenbein, Sophia Kitsiou, Ariadni Mavrou, et al.
Pageof 3

Showing results (1-10 of 27) with videos related to

Sort By:
Pageof 3
Turkish Journal of Orthodontics|April 4, 2022
Orofacial Manifestations Associated with Muscular Dystrophies: A ReviewPetros Papaefthymiou, Kyriaki Kekou, Fulya Özdemir
Movement Disorders : Official Journal of the Movement Disorder Society|September 27, 2016
Analysis of a founder mutation in the TH gene in a cohort of greek patients with Parkinson's diseaseRoser Pons, Kyriaki Kekou, Roubina Antonellou, et al.
The Journal of Molecular Diagnostics : JMD|February 26, 2010
SURVEYOR on the spot: strengths and weaknesses in molecular diagnosticsNikolaos Vogiatzakis, Kyriaki Kekou, Christalena Sophocleous, et al.
Molecular Biotechnology|August 13, 2013
Screening human genes for small alterations performing an enzymatic cleavage mismatched analysis (ECMA) protocolNikolaos Vogiatzakis, Kyriaki Kekou, Christalena Sophocleous, et al.
Neurology India|September 15, 2016
Myotonic dystrophy type 2 presenting as inflammatory myopathyConstantinos Papadopoulos, Grigoris Panagopoulos, Kyriaki Kekou, et al.
Neurology India|July 7, 2017
Author's Reply: Myotonic dystrophy: The occurrence of early-onset cataractConstantinos Papadopoulos, Grigoris Panagopoulos, Kyriaki Kekou, et al.
Molecular Biotechnology|October 24, 2007
Screening human genes for small alterations performing an enzymatic cleavage mismatched analysis (ECMA) protocolNikolaos Vogiatzakis, Kyriaki Kekou, Christalena Sophocleous, et al.
The Neurologist|July 18, 2015
Caveolinopathies in GreeceConstantinos Papadopoulos, George K Papadimas, Kyriaki Kekou, et al.
Pediatric Diabetes|November 13, 2021
Homozygosity of the Z-2 polymorphic variant in the aldose reductase gene promoter confers increased risk for neuropathy in children and adolescents with Type 1 diabetesDimitra Kallinikou, Charalampos Tsentidis, Kyriaki Kekou, et al.
Hormone Research|January 31, 2004
Tall stature, insulin resistance, and disturbed behavior in a girl with the triple X syndrome harboring three SHOX genes: offspring of a father with mosaic Klinefelter syndrome but with two maternal X chromosomesChristina Kanaka-Gantenbein, Sophia Kitsiou, Ariadni Mavrou, et al.
Pageof 3